Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs121913538
rs121913538
1 1.000 0.036 12 25245328 missense variant C/A,G snp 0.700 2 2014 2015
dbSNP: rs1764391
rs1764391
2 0.923 0.071 1 34795168 missense variant C/G,T snp 0.30 0.39 0.010 1.000 1 2010 2010
dbSNP: rs730882004
rs730882004
2 1.000 0.036 17 7674254 missense variant T/C snp 0.010 1.000 1 2011 2011
dbSNP: rs760881374
rs760881374
1 1.000 0.036 19 35721464 G/A,T snp 1.6E-05 3.2E-05; 3.2E-05 0.010 1.000 1 2015 2015